Tassabehji May, Hammond Peter, Karmiloff-Smith Annette, Thompson Pamela, Thorgeirsson Snorri S, Durkin Marian E, Popescu Nicholas C, Hutton Timothy, Metcalfe Kay, Rucka Agnes, Stewart Helen, Read Andrew P, Maconochie Mark, Donnai Dian
Academic Unit of Medical Genetics, University of Manchester, St. Mary's Hospital, Manchester M13 9PL, UK.
Science. 2005 Nov 18;310(5751):1184-7. doi: 10.1126/science.1116142. Epub 2005 Nov 3.
Craniofacial abnormalities account for about one-third of all human congenital defects, but our understanding of the genetic mechanisms governing craniofacial development is incomplete. We show that GTF2IRD1 is a genetic determinant of mammalian craniofacial and cognitive development, and we implicate another member of the TFII-I transcription factor family, GTF2I, in both aspects. Gtf2ird1-null mice exhibit phenotypic abnormalities reminiscent of the human microdeletion disorder Williams-Beuren syndrome (WBS); craniofacial imaging reveals abnormalities in both skull and jaws that may arise through misregulation of goosecoid, a downstream target of Gtf2ird1. In humans, a rare WBS individual with an atypical deletion, including GTF2IRD1, shows facial dysmorphism and cognitive deficits that differ from those of classic WBS cases. We propose a mechanism of cumulative dosage effects of duplicated and diverged genes applicable to other human chromosomal disorders.
颅面异常约占人类所有先天性缺陷的三分之一,但我们对控制颅面发育的遗传机制的理解并不完整。我们发现GTF2IRD1是哺乳动物颅面和认知发育的一个遗传决定因素,并且我们认为TFII-I转录因子家族的另一个成员GTF2I在这两个方面都有作用。Gtf2ird1基因敲除小鼠表现出的表型异常让人联想到人类微缺失疾病威廉姆斯-博伦综合征(WBS);颅面成像显示,颅骨和颌骨均存在异常,这可能是由于Gtf2ird1的下游靶点鹅膏蕈氨酸调控异常所致。在人类中,一名罕见的患有包括GTF2IRD1在内的非典型缺失的WBS个体,表现出与经典WBS病例不同的面部畸形和认知缺陷。我们提出了一种适用于其他人类染色体疾病的重复和分化基因累积剂量效应机制。